This product should not be sold or fed to pets. Pet owners should dispose of product in a safe manner (example, a securely covered trash receptacle) and return the empty bag to the store where purchased for a full refund.

Salmonella can cause serious infections in dogs and cats, and, if there is cross contamination caused by handling of the pet food, in people as well, especially children, the aged, and people with compromised immune systems. Healthy people potentially infected with Salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. On rare occasions, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms. Consumers exhibiting these signs after having contact with this product should contact their healthcare providers.

Pets with Salmonella infections may be lethargic and have diarrhea or bloody diarrhea, fever, and vomiting. Some pets will have only decreased appetite, fever and abdominal pain. Animals can be carriers with no visible symptoms and potentially infect other animals or humans. If your pet has consumed the recalled product and has these symptoms, please contact your veterinarian.

There have been no complaints or reports of illness resulting from consumption or handling of the recalled product.

Pet owners who have questions about the recall should call 1-877-568-4463 or visit www.petcare.mars.com.

  Recalled Pet Food
  Product: SPECIAL KITTY(R) Gourmet Blend Dry Cat Food
  Best If Used By Date: AUG 11 09
  Best If Used By Date Location: Back of bag

Production Lot Code: 50 XXXX X (Found on back of bag just after “Best If Used By” date. Consumers should look for “50″ as the first two digits of the second line.)

UPC Code: UPC code numbers can be found directly underneath the bar code on the package. Please find recalled pet food UPC information below.

  3.5 lb.      SPECIAL KITTY  (R) Gourmet Blend       81131 17546
  7 lb.        SPECIAL KITTY  (R) Gourmet Blend       81131 17547
  18 lb.       SPECIAL KITTY  (R) Gourmet Blend       81131 17548

Affected Stores: Wal-Mart locations in Connecticut, Delaware, Massachusetts, Maryland, Maine, North Carolina, New Hampshire, New Jersey, New York, Ohio, Pennsylvania, Rhode Island, Virginia, Vermont, and West Virginia.

In an effort to prevent the transmission of Salmonella from pets to family members and care givers, the FDA recommends that everyone follow appropriate pet food handling guidelines when feeding their pets. A list of safe pet food handling tips can be found at: www.fda.gov/consumer/updates/petfoodtips080307.html

Pet owners who have questions about the recall should call 1-877-568-4463 or visit www.petcare.mars.com.

Source: Mars Petcare US

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The products and lot numbers involved in the recall were produced at the Fremont, Neb., feed plant only, and are described as:

Lot numbers range from Jan. 1, 2008, to May 30, 2008, and are listed on the bag as 8JAN01FRE1 to 8MAY30FRE1 inclusive.

Lot numbers are printed on both the tag and sewing strip of each bag. Lot numbers are formatted as follows: Example 8MAY30FRE1 – 8=Year / MAY= Month / 30=Day of Month / FRE1=Plant Code.

The products included in this recall were distributed only in the following areas: Nebraska, north central Kansas, northwest Colorado, southern Minnesota, and western and south central Iowa.

The recall was initiated after receiving a customer complaint regarding the products. In addition, Land O’Lakes Purina Feed stopped producing the lamb feeds at the Fremont, Neb. plant and immediately began product testing.

To date, the presence of copper above acceptable levels has been found, which can cause serious health issues, and at high levels, mortality in sheep.

Retailers have been contacted to quarantine these products and notify customers who purchased the product. The affected product should not continue to be stored or used. Customers who purchased these products will receive replacement product.

For more information on the product recall, contact Customer Service at 1-877- 585-2365.

Source: FDA

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“This is the first veterinary drug to be marketed under a risk minimization and restricted distribution program. Numerous drugs for use in people have been successfully marketed under similar programs,” said Bernadette Dunham, D.V.M., Ph.D., director, FDA’s Center for Veterinary Medicine. “While we concur with the limited return of ProHeart 6 to the U.S. market, we strongly encourage veterinarians and pet owners to report any possible adverse reactions.”

Heartworm disease is a serious and potentially fatal condition for dogs. The parasite that causes heartworm disease is transmitted through the bite of a mosquito.

The risk minimization and restricted distribution program is intended to educate veterinarians and pet owners regarding the possible risks associated with the use of ProHeart 6. Therefore, Fort Dodge Animal Health is requiring veterinarians who wish to purchase ProHeart 6 to register with the company and participate in a Web-based training program prior to obtaining the product.

The return of ProHeart 6 to the market is based on results of additional toxicological and pharmacologic studies by Fort Dodge Animal Health coupled with the low adverse reaction frequency in international markets.

In 2004, Fort Dodge Animal Health agreed to voluntarily recall the product from the market based upon FDA’s concerns regarding reports of serious adverse reactions in dogs following the use of ProHeart 6. In response to FDA’s concerns, the manufacturer conducted additional testing of its product, which indicated that residues of the solvents used in the manufacture of ProHeart 6 may cause allergic reactions.

The manufacturer has improved the manufacturing specifications for ProHeart 6 to decrease the presence of those residues and has marketed the product in international markets. Few adverse events have been reported with this reformulated product.

The ProHeart 6 label and Client Information Sheet have been revised to include updated safety information. The new label includes warnings not to administer the drug within one month of vaccinations, and to use the product with caution in dogs with pre-existing allergic diseases including food allergies, allergic hypersensitivity, and flea allergy dermatitis. The label also warns against administering the drug to dogs who are sick, debilitated, underweight, or who have a history of weight loss. In addition, the label’s Post-Approval Experience section has been updated to include information about adverse reactions based on voluntary post-approval drug experience reporting.

Dog owners who suspect their dog is experiencing an adverse reaction to ProHeart 6 should immediately contact their veterinarian to initiate appropriate veterinary care. Veterinarians should contact Fort Dodge Animal Health to report any adverse events at (800) 533-8536.

Source: FDA

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Hartz recalled a specific lot code of Hartz Vitamin Care for Cats last November due to similar concerns. Both lot codes were manufactured for Hartz by UFAC (USA) Inc. in 2007, and were removed from distribution last November. However, bottles from the second lot had been shipped to customers prior to their having been removed from distribution.

Salmonella is an organism which can cause serious infections in young children, frail or elderly people, and others with weakened immune systems, all of whom are at particular risk from exposure and should avoid handling these products.

Salmonella symptoms may include fever, diarrhea, abdominal pain, and nausea in both cats and humans. Anyone experiencing the symptoms of Salmonella infection should seek immediate medical attention. Owners of cats exhibiting these symptoms should also seek veterinary assistance.

The product involved is 739 bottles of Hartz Vitamin Care for Cats, lot code SZ 22771, UPC number 32700-97701. While normal testing conducted by Hartz and UFAC has not revealed the presence of Salmonella in any Hartz products, recent sampling conducted by the FDA did detect the presence of Salmonella.

Although the company has not received any reports of animals or humans becoming ill as a result of coming into contact with this product, Hartz is taking immediate steps to recover this product from consumers. Cat owners should check the lot code on their bottles, and, if the code is not visible, or if the bottle has lot code SZ 22771 or lot code SZ-16371 imprinted thereon, they should immediately discontinue use of the product and discard it in a proper manner.

Consumers can contact Hartz at 1-800-275-1414 with any questions they may have and to obtain reimbursement for purchased product.

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